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Published on: February 28, 2013
Chemerin rs17173608 Gene Polymorphism is not Associated with Type 2 Diabetes Mellitus: a Cross-sectional Study
Serdar Olt1, Orhan Öznas1, Haydar Bağış2
1Department of Internal Medicine, Faculty of Medicine, Adıyaman University, Adıyaman, Turkey.
This study investigated the Chemerin rs17173608 gene polymorphism in type 2 diabetes mellitus (T2DM). While TT genotype ratios were higher in T2DM patients, no statistically significant differences were found between T2DM and control groups for genotypes or allele frequencies.
Area of Science:
- Genetics
- Metabolic Diseases
- Molecular Biology
Background:
- Chemerin plays a role in metabolic disorders like obesity, insulin resistance, metabolic syndrome, polycystic ovary syndrome (PCOS), and type 2 diabetes mellitus (T2DM).
- Investigating specific gene polymorphisms, such as Chemerin rs17173608, is crucial for understanding disease mechanisms.
Purpose of the Study:
- To examine the association between the Chemerin rs17173608 gene polymorphism and type 2 diabetes mellitus.
- To determine if this specific polymorphism influences T2DM risk or characteristics.
Main Methods:
- DNA was isolated from 100 T2DM patients and 50 healthy controls.
- Chemerin gene polymorphism (rs17173608) was analyzed using Tetra-Amplification Refractory Mutation System polymerase chain reaction (T-ARMS-PCR).
- Genotyping results were validated using sequence analysis and gel electrophoresis.
Main Results:
- The GG genotype for Chemerin rs17173608 was not detected in either T2DM patients or healthy controls.
- Genotype distribution showed TT and TG genotypes in both groups, with slightly higher TT ratios in T2DM patients.
- No statistically significant differences in genotype or G allele frequency were observed between the T2DM and control groups.
Conclusions:
- This is the first study to investigate the Chemerin rs17173608 gene polymorphism in relation to T2DM.
- Despite observed differences in genotype frequencies, the Chemerin rs17173608 polymorphism does not appear to be significantly associated with T2DM in the studied population.
- Further research with larger cohorts may be warranted to fully elucidate the role of chemerin in T2DM pathogenesis.
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